AccessGUDID - DEVICE: Dynatron Solaris Plus 707 (10660584000031)

GUDID

Device Identifier (DI) Information

Brand Name: Dynatron Solaris Plus 707
Version or Model: D717
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: Dynatronics Corporation

Primary DI Number: 10660584000031
Issuing Agency: GS1
Commercial Distribution End Date: October 31, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 113399125 *Terms of Use

Device Description: No description.

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
61186	Multi-modality physical therapy system, professional-use	An assembly of electrically-powered devices designed for professional use to apply multiple different energies (e.g., light-energy, ultrasound, radio-frequency electrical stimulation, electrotherapy) either alone or in sequence, but not simultaneously, to noninvasively treat/prevent a variety of soft-tissue, neuromuscular, and musculoskeletal injuries/disorders (e.g., joint pain/inflammation, stiffness, soft tissue injuries, muscle atrophy); it may in addition be used for aesthetic skin/body contouring (e.g., minimize cellulite, loose or wrinkled skin). It consists of a multi-modality control unit/generator, and dedicated applicators for the transcutaneous delivery of energy.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LIH	Interferential Current Therapy
IPF	Stimulator, Muscle, Powered
ILY	Lamp, Infrared, Therapeutic Heating
GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K031329	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between -40 and 70 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Weight: 8.2 Pound
Height: 4.0 Inch
Width: 18.5 Inch
Length: 12.0 Inch

Device Record Status

Public Device Record Key: 2d4b6c09-4a8d-4ade-b81b-f97862d4dc2d
Public Version Date: April 18, 2025
Public Version Number: 7
DI Record Publish Date: September 24, 2016